Canonical Allele Identifier: CA723143313
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1409429350
gnomAD v3: 16-68829498-T-C
gnomAD v4: 16-68829498-T-C
MyVariant Identifiers: chr16:g.68863401T>C (hg19) chr16:g.68829498T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829498T>C , CM000678.2:g.68829498T>C GRCh38
NC_000016.9:g.68863401T>C , CM000678.1:g.68863401T>C GRCh37
NC_000016.8:g.67420902T>C NCBI36
NG_008021.1:g.97207T>C , LRG_301:g.97207T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2296-156T>C MANE Select ENSP00000261769.4:n.2296-156T>C
ENST00000261769.9:c.2296-156T>C ENSP00000261769.4:n.2296-156T>C
ENST00000422392.6:c.2113-156T>C ENSP00000414946.2:n.2113-156T>C
ENST00000562118.1:n.514-156T>C
ENST00000562836.5:n.2367-156T>C
ENST00000566510.5:c.*962-156T>C ENSP00000458139.1:n.*962-156T>C
ENST00000566612.5:c.*536-156T>C ENSP00000454782.1:n.*536-156T>C
ENST00000611625.4:c.2359-156T>C ENSP00000481063.1:n.2359-156T>C
ENST00000612417.4:c.1853+2944T>C ENSP00000478360.1:n.1853+2944T>C
ENST00000621016.4:c.1866-4705T>C ENSP00000480664.1:n.1866-4705T>C
NM_004360.3:c.2296-156T>C , LRG_301t1:c.2296-156T>C NP_004351.1:n.2296-156T>C
XM_011523488.1:c.1561-156T>C XP_011521790.1:n.1561-156T>C
XM_011523489.1:c.1561-156T>C XP_011521791.1:n.1561-156T>C
NM_001317184.1:c.2113-156T>C NP_001304113.1:n.2113-156T>C
NM_001317185.1:c.748-156T>C NP_001304114.1:n.748-156T>C
NM_001317186.1:c.331-156T>C NP_001304115.1:n.331-156T>C
NM_004360.4:c.2296-156T>C NP_004351.1:n.2296-156T>C
NM_004360.5:c.2296-156T>C MANE Select NP_004351.1:n.2296-156T>C
NM_001317184.2:c.2113-156T>C NP_001304113.1:n.2113-156T>C
NM_001317185.2:c.748-156T>C NP_001304114.1:n.748-156T>C
NM_001317186.2:c.331-156T>C NP_001304115.1:n.331-156T>C
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